Canonical Allele Identifier: CA25066759
Gene: LINC02238 HGNC NCBI

Linked Data

dbSNP Id: rs12145291
gnomAD v2: 1-74161795-T-C
gnomAD v3: 1-73696112-T-C
gnomAD v4: 1-73696112-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.73696112T>C , CM000663.2:g.73696112T>C GRCh38
NC_000001.10:g.74161795T>C , CM000663.1:g.74161795T>C GRCh37
NC_000001.9:g.73934383T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_146300.1:n.99-3639T>C